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  3. GALA-chol

GALA-chol is a cholesterol-conjugated pH-responsive fusion peptide that can serve as a delivery adjuvant. GALA-chol enhances the endocytosis of siRNA RET/PTC1-SQ nanoparticles, inhibits cell viability, and undergoes pH-responsive charge conversion in the acidic lysosomal environment, thereby promoting lysosomal escape of small extracellular vesicle (sEV) cargo. GALA-chol anchors to the sEV membrane and maintains the structural integrity and intrinsic homing activity of sEVs. GALA-chol can be used in studies related to adjuvant delivery.

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GALA-chol

GALA-chol Chemical Structure

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Description

GALA-chol is a cholesterol-conjugated pH-responsive fusion peptide that can serve as a delivery adjuvant. GALA-chol enhances the endocytosis of siRNA RET/PTC1-SQ nanoparticles, inhibits cell viability, and undergoes pH-responsive charge conversion in the acidic lysosomal environment, thereby promoting lysosomal escape of small extracellular vesicle (sEV) cargo. GALA-chol anchors to the sEV membrane and maintains the structural integrity and intrinsic homing activity of sEVs. GALA-chol can be used in studies related to adjuvant delivery[1][2].

In Vitro

Nanoparticles composed of GALA-Chol (10% proportion) and 50 nM siRNA RET/PTC1-SQ reduce the viability of BHP 10-3 SC mice and TPC-1 cells by approximately 20% at 48 h and 72 h (treatment duration: 24-72 h), and the inhibitory effect is enhanced (by approximately 50%) when combined with Lipofectamine 2000[1].
Nanoparticles composed of GALA-Chol and siRNA RET/PTC1-SQ (10% GALA-Chol; 50 nM siRNA; 24-48 h) significantly inhibit the expression of RET/PTC1 gene and protein in BHP 10-3 SC mice and TPC-1 cells at both 24 h and 48 h, whereas siRNA RET/PTC1-SQ nanoparticles without GALA-Chol exhibit no silencing activity[1].
Nanoparticles composed of GALA-Chol and siRNA RET/PTC1-SQ (10% GALA-Chol; 50 nM siRNA; 4 h) are efficiently internalized by BHP 10-3 SCmice cells, while siRNA RET/PTC1-SQ nanoparticles without GALA-Chol cannot cross the cell membrane[1].
After functional modification of sEVs derived from MCF-7 cells with GALA-chol (0-10 μM/109 sEV particles), the cytoplasmic cargo delivery efficiency to MCF-7 cells reaches the maximum at a concentration of 8 μM/109 particles; at higher concentrations, the delivery efficiency decreases due to steric hindrance interference[2].
MCF-7-derived sEVs functionalized with GALA-chol (8 μM/109 sEV particles; 0-10 h) enable efficient lysosomal escape of cargo in MCF-7 cells after 6 h of incubation, showing a significant increase in cytoplasmic cargo distribution compared with non-functionalized sEVs[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: BHP 10-3 SCmice, TPC-1 (human papillary thyroid carcinoma cell lines harboring RET/PTC1 fusion oncogene)
Concentration: 10% molar ratio of GALA-Chol relative to siRNA RET/PTC1-SQ; 50 nM siRNA concentration
Incubation Time: 24 h, 48 h, 72 h
Result: Inhibited cell viability by ~10% at 24 h and ~20% at 48 h and 72 h compared to untreated cells.
Enhanced inhibition to ~50% when combined with Lipofectamine 2000.
Molecular Weight

3603.23

Formula

C170H269N35O48S

Sequence

Ac-Trp-Glu-Ala-Ala-Leu-Ala-Glu-Ala-Leu-Ala-Glu-Ala-Leu-Ala-Glu-His-Leu-Ala-Glu-Ala-Leu-Ala-Glu-Ala-Leu-Glu-Ala-Leu-Ala-Ala-{Cys(cholesterol)}-NH2

Sequence Shortening

Ac-WEAALAEALAEALAEHLAEALAEALEALAA-{Cys(cholesterol)}--NH2

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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GALA-chol
Cat. No.:
HY-P11766
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